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Symbol
Name
ID

Ocln
occludin
MGI:106183

Phenotype annotations related to skeleton

Darker colors indicate more annotations

Human Phenotypes	Microretrognathia	Microcephaly	Cerebral calcification
Disease(s) Associated with OCLN
pseudo-TORCH syndrome 1

Mouse Phenotypes		abnormal femur morphology	abnormal trabecular bone morphology
Availability	Mouse Genotype	abnormal femur morphology	abnormal trabecular bone morphology
	Ocln^{Gt(ROSA)39Tshi}/Ocln^{Gt(ROSA)39Tshi}
	Ocln^tm1Sts/Ocln^tm1Sts
	Ocln^tm1Tshi/Ocln^tm1Tshi
	Ocln^tm2Sts/Ocln^tm2Sts

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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